• You are responsible for the implementation of global studies in Germany. • Study management: You are responsible for a selection of studies — from site selection through conduct to close-out. • Coordination: You work closely with your local CRA colleagues across various study teams and contribute to timely project delivery through proactive planning. • Monitoring: You oversee a selection of investigational sites and monitor collaborations with partners and authorities as well as overall site management together with your local CRA colleagues. • Compliance: You ensure that all internal and external requirements are met in your projects and that sites are inspection-ready at all times.

• You are responsible for implementing global studies in Germany • You work closely with your local CRA colleagues within various study teams • You oversee a selection of investigational sites and manage collaboration with partners and regulatory authorities • You ensure that all internal and external requirements and standards are met in your projects

• Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance. • Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials. • Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience. • Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol and monitoring plans, in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards. • Gather local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy. • Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey. • Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance. • Possesses experienced level of competency to mentor and train less experienced CRAs on various aspects of work and provides input into their development. • Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues. • Identifies, evaluates and recommends new/potential investigators/sites on an on going basis.

• Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients • Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials • Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience • Considered as the primary point of contact for the investigative site, provides contextual information on the clinical trials, connects stakeholder to the investigative sites and strengthens AbbVie’s positioning • Aligns, trains and motivates the site staff and principal investigator under supervision on the goals of the clinical trial program, protocol, and patient treatment principles for the trial ensuring a trusted partnership • Conducts site evaluation, site training, routine, and site closure monitoring activities under supervision, in compliance to the protocol and monitoring plans and accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and to quality standards in conducting clinical research, ensuring safety and protection of study subjects • Customize site engagement strategy for assigned study (ies) under supervision • Gather local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy • Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey • Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues • Ensures preventative and corrective action plans are put into place, as needed, to mitigate risk and promote compliance